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MRI and CT findings of isolated intracranial Rosai–Dorfman disease in a child
Isolated intracranial Rosai–Dorfman disease (RDD) is extremely rare in pediatric patients. We present the case of a 22-month-old boy whom had isolated intracranial RDD involvement. To our knowledge, a parieto-occipital regional involvement without a dural tail sign has not been previously documented...
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| Vydáno v: | Neuroradiol J |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
SAGE Publications
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4978314/ https://ncbi.nlm.nih.gov/pubmed/26915894 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1971400915628020 |
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